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花生转录因子LEC1的表达特性分析 被引量:2

Analysis on Expression of the Transcription Factor LEC1 in Peanut
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摘要 LEC1是调控植物胚形成和发育的重要转录因子。本研究根据已获得的花生AhLEC1基因序列,利用原核表达分析和实时荧光定量PCR(qRT-PCR)技术初步验证其在花生中的生物学功能。结果表明:①原核表达分析显示,获得了分子量为25 kD左右的目的蛋白条带,与预期大小一致。②组织表达分析显示,AhLEC1基因在花生的花及果针中微量表达,在荚果以及种子发育过程有明显的时序表达特性。AhLEC1基因在荚果发育过程中出现先增后降的趋势,在种子发育的前期表达量高,后期逐渐降低。③非生物胁迫表达分析显示,AhLEC1基因在低温、高盐以及干旱处理的花生叶片中表达量明显上调,表明AhLEC1基因可能参与花生对非生物胁迫的抗性调控。 LEC1 is an important transcription factor regulating the formation and development of plant embryo.In this study,based on the obtained peanut AhLEC1 gene sequence,the prokaryotic expression analysis and real-time fluorescence quantitative PCR(qRT-PCR)technology were used to preliminarily verify its biological function in peanut.The results showed that:①Prokaryotic expression analysis showed that a target protein band with a molecular weight of about 25 kD was obtained,which was consistent with the expected size.②Tissue expression analysis showed that the AhLEC1 gene was slightly expressed in peanut flower and peg,and had obvious temporal expression characteristics during pod and seed development process.The AhLEC1 gene showed a trend of increasing at first and then decreasing during the pod development.The expression level of AhLEC1 gene was high in the early stage of seed development and gradually decreased in the later stage.③Abiotic stress expression analysis showed that the expression of AhLEC1 gene was significantly up-regulated in peanut leaves treated with low temperature,high salt and drought,indicating that the AhLEC1 gene may be involved in the regulation of peanut resistance to abiotic stress.
作者 潘丽娟 王冕 苏茂文 陈明娜 王通 许静 杨珍 孙伟 邹宗峰 禹山林 陈娜 迟晓元 PAN Li-juan;WANG Mian;SU Mao-wen;CHEN Ming-na;WANG Tong;XU Jing;YANG Zhen;SUN Wei;ZOU Zong-feng;YU Shan-lin;CHEN Na;CHI Xiao-yuan(Shandong Peanut Research Institute,Qingdao 266100,China;Qingdao Customs,Qingdao 266001,China;Linyi Academy of Agricultural Sciences,Linyi 276012,China;Yantai Agricultural Technology Extension Center,Yantai 264001,China)
出处 《花生学报》 北大核心 2021年第2期15-20,共6页 Journal of Peanut Science
基金 国家自然科学基金项目(31701464) 国家花生产业技术体系项目(CARS-13) 泰山学者工程专项(tsnq201812121) 山东省农业科学院农业科技创新工程(CXGC2016B02,CXGC2018E21) 山东省重大科技创新工程项目(2019JZZY010702) 广东省重点领域研发计划项目(2020B020219003) 临沂市重点研发计划(2019YD009) 青岛市科技惠民示范引导专项(20-3-4-26-nsh) 山东省自然科学基金项目(ZR2020MC103)。
关键词 花生 AhLEC1基因 原核表达 实时荧光定量PCR 基因表达特性 peanut AhLEC1 gene prokaryotic expression qRT-PCR gene expression characteristics
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  • 1仇键,谭晓风.植物种子油体及相关蛋白研究综述[J].中南林学院学报,2005,25(4):96-100. 被引量:18
  • 2程红焱,宋松泉.种子的贮油细胞器——油体及其蛋白[J].植物学通报,2006,23(4):418-430. 被引量:31
  • 3MEINKE D W,FRANZMANN L H,NICKLE T C,et al.Leafy cotyledon mutants of Arabidopsis[J].Plant Cell, 1994 ( 6 ) : 1049-1064.
  • 4WEST M, MATSUDAIRA Y K, DANAO J, et al.LEAFY COTYLEDON 1 " is an essential regulator of late embryogenesis and cotyledon identity in Arabidopsis[J].Plant Cell, 1994 ( 6 ) : 1731 - 1745.
  • 5PARCY-F,VALON C,KOHARA A.The ABSCISIC ACIDINSENSITIVE3,FUSCA3,and LEAFY COTYLEDON1 Loci Act in Concert to Control Multiple Aspects of Arabidopsis Seed Development[J].Plant Cell, 1997(9) : 1265-1277.
  • 6LOTAN T,OHTO M ,MATSUDAIRA YEE K,et al. Arabidopsis LEAFY COTYLEDON1 is sufficient to induce embryo development in vegetative cells[J].Cell, 1998,93 ( 6 ) : 1195-1205.
  • 7YAZAWA K,TAKAHATA K, KAMADA H. Isolation of the gene encoding Carrot leafy cotyledonl and expression analysis during somatic and zygotic embryogenesis[J].Plant Physiol Biochem, 2004,42 ( 3 ) : 215-225.
  • 8ZHANG S, WONG L, MENG L, et al. Similarity of expression patterns of knottedl and ZmLEC1 during somatic and zygotic embryogenesis in maize(Zea mays L.)[J].Planta,2002,215(2) : 191-194.
  • 9FAMBRINI M, DURANTE C, CIONINI G,et al.Characterization of LEAFY COTYLEDON1-LIKE gene in Helianthus annuus and its relationship with zygotic and somatic embryogenesis[J].Development genes and evolution, 2006,216 (5) : 253-264.
  • 10KWONG R W,BUI Q,LEE H,et al. LEAFY COTYLEDON1-LIKE A defines a class of regulators essential for embryo development [J].Plant Cell,2003 (15) :5-18.

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